| Literature DB >> 24842479 |
Toru Sakairi1, Satoshi Okabe1, Keiju Hiromura1, Shinsuke Motegi1, Noriyuki Sakurai1, Hidekazu Ikeuchi1, Yoriaki Kaneko1, Akito Maeshima1, Junko Hirato2, Yoshihisa Nojima1.
Abstract
A 62-year-old male patient presented with progressive renal dysfunction for 2 months. He had elevated serum C-reactive protein and IgG4 levels with absence of anti-neutrophil cytoplasmic antibodies. A renal biopsy showed severe tubulointerstitial nephritis (TIN) with extensive infiltration of IgG4-positive plasma cells, suggesting a diagnosis of IgG4-related kidney disease (IgG4-RKD). However, the identification of a few crescentic glomeruli and necrotizing vasculitis of an interlobular artery lead to a diagnosis of renal small-vessel vasculitis. This case indicates that a careful examination is required to distinguish between IgG4-RKD and TIN caused by renal small-vessel vasculitis.Entities:
Keywords: ANCA-associated vasculitis; IgG4-related disease; Renal small-vessel vasculitis; Tubulointerstitial nephritis
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Year: 2014 PMID: 24842479 DOI: 10.3109/14397595.2014.915510
Source DB: PubMed Journal: Mod Rheumatol ISSN: 1439-7595 Impact factor: 3.023